NM_000546.6:c.469G>A

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HGVS Expressions

  • NG_017013.2:g.17408G>A
  • NM_000546.6:c.469G>A
  • NP_000537.3:p.Val157Ile

Associated Genes

Tumor Protein p53
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Genomic Location

chr17:7675143

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

121912654

Clinvar

185404

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.60LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'D8' from family 31 in the publi...
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Contributors

  • Asha Deepthi: 06.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 06.09.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.